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AutoPulse Assisted Prehospital International Resuscitation Trial (ASPIRE)

NCT00120965 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1837

Last updated 2011-01-27

No results posted yet for this study

Summary

The AutoPulse Assisted Prehospital International Resuscitation (ASPIRE) Trial compares the efficacy of circulatory assist by manual chest compression versus an automated chest compression device (AutoPulse™) during the resuscitative attempt following out-of-hospital cardiac arrest.

Conditions

  • Cardiac Arrest

Interventions

DEVICE

AutoPulse

Standard device settings

OTHER

Manual CPR

Manual CPR

Sponsors & Collaborators

Principal Investigators

  • Alfred P. Hallstrom, PhD · University of Washington

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-06-30
Completion
2005-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00120965 on ClinicalTrials.gov